RAGE: a single receptor fits multiple ligands

被引:349
作者
Fritz, Guenter [1 ]
机构
[1] Univ Freiburg, Dept Neuropathol, Neurozentrum, D-79106 Freiburg, Germany
关键词
GLYCATION END-PRODUCTS; INFLAMMATORY CELL RECRUITMENT; STRUCTURAL BASIS; S100; PROTEINS; NEURONAL DIFFERENTIATION; PATTERN-RECOGNITION; ALZHEIMERS-DISEASE; CYTOPLASMIC DOMAIN; CRYSTAL-STRUCTURE; ENDPRODUCTS RAGE;
D O I
10.1016/j.tibs.2011.08.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The receptor for advanced glycation end products (RAGE) is a central signaling molecule in the innate immune system and is involved in the onset and sustainment of the inflammatory response. RAGE belongs to a class of pattern recognition receptors that recognize common features rather than a specific ligand. Recent structural information on the extracellular portion (ectodomain) of RAGE shed new light on this unusual ability. X-ray crystallographic, NMR and biochemical data suggest that ligand binding is driven largely by electrostatic interactions between the positively charged surface of the ectodomain and negatively charged ligands. In this article, I propose a putative mechanism of RAGE ligand recognition of receptor activation.
引用
收藏
页码:625 / 632
页数:8
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